TY - JOUR
T1 - The Mystery of Antibodies Against Polyethylene Glycol (PEG) - What do we Know?
AU - Lubich, Christian
AU - Allacher, Peter
AU - de la Rosa, Maurus
AU - Bauer, Alexander
AU - Prenninger, Thomas
AU - Horling, Frank Michael
AU - Siekmann, Jürgen
AU - Oldenburg, Johannes
AU - Scheiflinger, Friedrich
AU - Reipert, Birgit Maria
N1 - Publisher Copyright:
© 2016, Springer Science+Business Media New York.
PY - 2016/9/1
Y1 - 2016/9/1
N2 - Purpose: Recent findings demonstrated anti-PEG antibody formation in some healthy individuals and patients who have not received PEGylated biotherapeutics. Some of these findings evoked criticism because of shortcomings in the antibody assays used. To better understand this topic, we established robust antibody analytics and screened two cohorts of healthy individuals and one cohort of hemophilia patients for the expression of anti-PEG antibodies. Methods: A flow cytometry approach and a fully validated ELISA platform were established to detect specific anti-PEG antibodies. Immunohistochemistry was used to test for potential binding of anti-PEG antibodies to human tissues. Results: IgM and/or IgG anti-PEG antibodies are expressed by some healthy individuals and by some patients with hemophilia who have not received PEGylated biotherapeutics. These antibodies can be either transient or persistent and recognize PEGs of different sizes with or without terminal methoxy groups. Age and location of healthy individuals influence the prevalence of IgG but not of IgM antibodies. Anti-PEG antibodies do not cross-react with human tissues supporting the safety of the antibodies. Conclusion: We confirm that some healthy individuals and some patients with hemophilia express specific antibodies against PEG which are not associated with any pathology and do not bind to human tissues.
AB - Purpose: Recent findings demonstrated anti-PEG antibody formation in some healthy individuals and patients who have not received PEGylated biotherapeutics. Some of these findings evoked criticism because of shortcomings in the antibody assays used. To better understand this topic, we established robust antibody analytics and screened two cohorts of healthy individuals and one cohort of hemophilia patients for the expression of anti-PEG antibodies. Methods: A flow cytometry approach and a fully validated ELISA platform were established to detect specific anti-PEG antibodies. Immunohistochemistry was used to test for potential binding of anti-PEG antibodies to human tissues. Results: IgM and/or IgG anti-PEG antibodies are expressed by some healthy individuals and by some patients with hemophilia who have not received PEGylated biotherapeutics. These antibodies can be either transient or persistent and recognize PEGs of different sizes with or without terminal methoxy groups. Age and location of healthy individuals influence the prevalence of IgG but not of IgM antibodies. Anti-PEG antibodies do not cross-react with human tissues supporting the safety of the antibodies. Conclusion: We confirm that some healthy individuals and some patients with hemophilia express specific antibodies against PEG which are not associated with any pathology and do not bind to human tissues.
KW - anti-PEG antibodies in healthy individuals
KW - anti-PEG antibodies in hemophilia patients
KW - human tissue cross-reactivity study
KW - PEGylated proteins
KW - specificity of anti-PEG antibodies
UR - http://www.scopus.com/inward/record.url?scp=84976314592&partnerID=8YFLogxK
U2 - 10.1007/s11095-016-1961-x
DO - 10.1007/s11095-016-1961-x
M3 - Article
C2 - 27271335
AN - SCOPUS:84976314592
SN - 0724-8741
VL - 33
SP - 2239
EP - 2249
JO - Pharmaceutical Research
JF - Pharmaceutical Research
IS - 9
ER -